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STICH3C Cardiac Magnetic Resonance (CMR) Observational Study (STICOS)
STICOS will test the hypothesis that residual jeopardized myocardium, late gadolinium enhancement, and non-ischemic substrate after revascularization is associated with postoperative adverse cardiovascular events such as heart failure , readmission, or death. This study will look at whether certain heart tissue abnormalities seen on MRI scans can help predict serious health problems after heart procedures like stents or bypass surgery.
iLVSD (ischemic left ventricular dysfunction) is a leading cause of heart failure (HF) and death. It is widely treated via coronary revascularization despite limited understanding of determinants of revascularization response. "Viability" imaging (to differentiate infarcted from salvageable myocardium) has been widely touted as an effective means to predict revascularization response. However prior multicenter trials have derived negative conclusions using heterogenous data with respect to both image modality and analysis. Data by our investigators and others indicate that infarct transmurality on CMR strongly impacts remodeling and prognosis after coronary revascularization. The investigators have also developed new methods (dark-blood late gadolinium enhancement-CMR) to assess infarction and shown ischemia (hypoperfusion) and non-ischemic substrate on CMR to strongly impact LV remodeling. Despite conceptual rationale, utility of multiparametric CMR to elucidate mechanism and determinants of remodeling and differential outcomes after percutaneous and surgical revascularization of iLVSD has yet to be tested. This prospective study will test the hypothesis that residual jeopardized (viable but hypoperfused) myocardium, LGE, and non-ischemic substrate after coronary revascularization (by PCI or CABG) is associated with postoperative adverse cardiovascular events
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
NewYork-Presbyterian Brooklyn Methodist Hospital
Brooklyn, New York, United States
New York Presbyterian - Queens
Flushing, New York, United States
Weill Cornell Medicine/NewYork Presbyterian Hospital
New York, New York, United States
MU Vienna Austria
Vienna, Austria
Libin Cardiovascular Institute
Calgary, Alberta, Canada
Universite Laval Quebec (CRIUCPQ) Canada
Québec, Canada
Sunnybrook Health Sciences Centre
Toronto, Canada
Ruijin Hospital Shanghai Jiao Tong University School of Medicine
Shanghai, China
Dedinje Cardiovascular Institute
Belgrade, Serbia
Start Date
March 1, 2024
Primary Completion Date
August 1, 2028
Completion Date
January 1, 2030
Last Updated
August 21, 2025
200
ESTIMATED participants
Cardiac Magnetic Resonance Imaging
DIAGNOSTIC_TEST
Lead Sponsor
Weill Medical College of Cornell University
Collaborators
NCT01311323
NCT01881555
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
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